Understanding gene mutations in childhood eye disease
Researcher Roly Megaw, a clinical lecturer and honorary consultant ophthalmologist from the University of Edinburgh and West Lothian joins us for this webinar. Roly will be shedding light on the devastating impact of RPGR gene mutations, which can cause macular and cone rod dystrophies. Join us as he unveils discoveries from his joint Macular Society and Retina UK-funded research, aiming improve our understanding of these conditions and find potential treatments.

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Investigating the genetics of RPGR-associated cone dystrophy with Cristina Martinez

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Retina की genetic बीमारी, Stargardt Disease. क्या हो जाते हैं total blind ? क्या कोई इलाज है ?

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